FDA Adverse Events Reporting System Drug Reaction 2018

The FDA Adverse Event Reporting System (FAERS) contains information on medication errors, quality complaints and drug-related adverse events that were submitted to FDA (U.S. Food and Drug Administration) in 2018. The drug reaction dataset contains all "Medical Dictionary for Regulatory Activities" (MedDRA) terms coded for the adverse event (1 or more).

美国食品药品监督管理局（FDA）的不良事件报告系统（FAERS）收录了2018年提交给FDA的药物错误、质量投诉以及药物相关的不良事件信息。该药物反应数据集包含所有针对不良事件（1个或多个）进行编码的“监管活动医学词典”（MedDRA）术语。